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Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992

[Pathology of unstable sequence of genome: fragile-X-syndrome]C Beldjord, L Richard

Annales De Genetique|January 1, 1995

Diagnostic usefulness of the polymorphism of the GT dinucleotide and the polythymidine tract in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneC Cazeneuve, C Beldjord, J C Kaplan, et al.

Human Mutation|January 1, 1995

Mutation heterogeneity of cystic fibrosis in France: screening by denaturing gradient gel electrophoresis using psoralen-modified oligonucleotideT Bienvenu, C Cazeneuve, J C Kaplan, et al.

Fertility and Sterility|February 24, 2000

A novel, rapid, and accurate method for detecting microdeletion involving the DAZ gene in infertile menH Lucas, C Patrat, P Jouannet, et al.

The Journal of Experimental Medicine|July 1, 1993

Peripheral selection of V delta 1+ cells with restricted T cell receptor delta gene junctional repertoire in the peripheral blood of healthy donorsK Beldjord, C Beldjord, E Macintyre, et al.

Clinical Endocrinology|January 7, 1999

Overexpression of vasopressin (V3) and corticotrophin-releasing hormone receptor genes in corticotroph tumoursY de Keyzer, P René, C Beldjord, et al.

Human Biology|February 1, 1992

Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplificationT Bienvenu, P Sebillon, D Labie, et al.

Nucleic Acids Research|September 11, 1995

A T to G mutation in the polypyrimidine tract of the second intron of the human beta-globin gene reduces in vitro splicing efficiency: evidence for an increased hnRNP C interactionP Sébillon, C Beldjord, J C Kaplan, et al.

Hormone Research|January 1, 1997

Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomasP Rodien, X Jeunemaitre, C Dumont, et al.

Journal of Intellectual Disability Research : JIDR|April 16, 1998

Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West IndiesA Elbaz, J Suédois, M Duquesnoy, et al.

Pageof 8

Showing results (1-10 of 77) with videos related to

Sort By:

Pageof 8

Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992

[Pathology of unstable sequence of genome: fragile-X-syndrome]C Beldjord, L Richard

Annales De Genetique|January 1, 1995

Diagnostic usefulness of the polymorphism of the GT dinucleotide and the polythymidine tract in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneC Cazeneuve, C Beldjord, J C Kaplan, et al.

Human Mutation|January 1, 1995

Mutation heterogeneity of cystic fibrosis in France: screening by denaturing gradient gel electrophoresis using psoralen-modified oligonucleotideT Bienvenu, C Cazeneuve, J C Kaplan, et al.

Fertility and Sterility|February 24, 2000

A novel, rapid, and accurate method for detecting microdeletion involving the DAZ gene in infertile menH Lucas, C Patrat, P Jouannet, et al.

The Journal of Experimental Medicine|July 1, 1993

Peripheral selection of V delta 1+ cells with restricted T cell receptor delta gene junctional repertoire in the peripheral blood of healthy donorsK Beldjord, C Beldjord, E Macintyre, et al.

Clinical Endocrinology|January 7, 1999

Overexpression of vasopressin (V3) and corticotrophin-releasing hormone receptor genes in corticotroph tumoursY de Keyzer, P René, C Beldjord, et al.

Human Biology|February 1, 1992

Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplificationT Bienvenu, P Sebillon, D Labie, et al.

Nucleic Acids Research|September 11, 1995

A T to G mutation in the polypyrimidine tract of the second intron of the human beta-globin gene reduces in vitro splicing efficiency: evidence for an increased hnRNP C interactionP Sébillon, C Beldjord, J C Kaplan, et al.

Hormone Research|January 1, 1997

Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomasP Rodien, X Jeunemaitre, C Dumont, et al.

Journal of Intellectual Disability Research : JIDR|April 16, 1998

Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West IndiesA Elbaz, J Suédois, M Duquesnoy, et al.

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